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Mental Health

We are being lured by the siren song of cynicism. We have to choose a different route.

We are being lured by the siren song of cynicism. We have to choose a different route.
Photo by Inu Etc on Unsplash

We can't let ourselves be lured by the siren song of cynicism.

"Why do people have to suck so badly?" my teen asks me after watching a viral video of horrible human behavior.

I understand the sentiment. I really do. I've asked myself the same question many times in recent years. Why are people like this? What is wrong with people? How can people be so stupid/cruel/selfish/ignorant/etc. And every time I have to pause, reflect and recognize what I'm hearing.

It's the siren song of cynicism. That strangely alluring voice that lulls us into a negative state of complacency at best and abject nihilism at worst.

I see—and feel in myself—cynicism as a natural, reactionary response to the ugly realities of our world, but also to our current digital climate. So much of the discouse we consume is filtered through social media algorithms that reward undernuanced hot takes and keep the cycle of negative sensationalism churning. The bad stuff gets our attention, which prompts people to talk about the bad stuff, which triggers algorithms that push more of the bad stuff, which creates a feedback loop informing us that everything is terrible.


Cynicism seduces us because it's easy. It doesn't actually feel good, but it feels comfortable because it doesn't ask anything from us. Hardened cynics sometimes see themselves as the intellectually honest among us, having real insight into people and problems, but it's simply not true. Cynicism requires no deep digging, real reflection or soul searching. It's the easiest thing in the world to call the world a dumpster fire, toss up our hands and say, "Welp, everything and everyone sucks, so what's the point?"

Hope, on the other hand, is hard. It requires going beyond our impulsive reactions to headlines and soundbites and to enage with humanity holistically. Far from being some kind of unthinking, Pollyanna-ish, head-in-the-sand idealism, I see hope as the natural outcome of truly diving into the reality of human existence.

But how do we get there? How do we ignore the pull of cynicism and navigate toward hope instead?

First, we can look to the past to see how far we have actually come.

I was watching the Olympics the other night and marveling at what human beings have figured out how to do. We started off rubbing sticks together to make fire. Now we have people who can artistically dance around on ice, spin multiple times through the air with the utmost perfection and precision, and land on one foot on a 1/8-inch blade. Not only that, but they do it to beautiful music that humans have composed, with musical instruments humans created, recorded on technological equipment that humans invented.

Not only was I watching this marvel happen, but I was doing so all the way on the other side of the planet, in the comfort of my home, where hot air blows out of the walls, clean water pours out of the refrigerator that keeps our food cold and lights turn on and off with the flick of a finger.

And that's just the basic, everyday life stuff we've figured out. Thinking of all of the ways humans continue to advance and progress is mind-boggling.

Sure, we still separate ourselves into artificial groups and fight over stupid things, but we also have created global organizations that collaborate to do incredible work to solve problems. Yes, our advancements have caused an imbalance in our relationship to the planet, but we also have developed the science to understand and begin to mitigate those impacts. Indeed, people can still be bafflingly ignorant or closed-minded, but we have access to everything that humans have ever learned available at our fingertips. That's incredible.

Our material progress may have outpaced our collective spiritual progress, and our political will to enact workable solutions might be a mess, but there's no reason to believe we won't figure those things out too. Look at all that we've been through and what we've accomplished. We are far more capable than we give ourselves credit for, in all areas.

Second, we can choose the filters with which we view the present.

When we look at the challenges we face and the difficulties in meeting those challenges, do we see a sign that humans are inept or a sign that we're trying to figure things out? Learning and problem-solving are messy, nonlinear processes. Sometimes progress is two steps forward, one step back. Growth involves growing pains, especially when we're actually growing the fastest. Building something new often requires tearing down something old first, and destruction feels like destruction even when it's necessary.

There's also the simple truth that we find what we look for. If we look for what is bad, wrong and unjust in the world, we'll find it. That stuff is there, no question. And some of it definitely needs our attention; ignoring a problem doesn't make it go away. But focusing on the negative all the time is a choice—one that doesn't serve anyone well.

I could easily spend an entire day finding examples of how people are awful, how it seems like we're going backward in some ways, how society is totally messed up and how the future is doomed. (Just spend the day on Twitter. It's all there.) If my goal were to justify a cynical outlook on humanity, I could easily do so.

But I could also spend an entire day finding examples of how humans are amazing, how people come together to help one another, how organizations are solving problems and providing for people's needs, how progress is being made in all fields of human endeavor. If my goal were to justify a hopeful vision for humanity, I could easily do that as well.

Each of those scenarios is a choice. Which day seems like it would lead to a better outcome, either for me personally or for the world at large?

The negative, cynical stuff is constantly in our faces because of how media and social media work, but the positive, constructive stuff is all around us. We need to balance positivity with addressing real problems, but when we put more focus and energy into supporting and amplifying the things we want to see than the things we don't, we steer our ship toward hope.

Finally, we can remember that the future is still unwritten.

One of the hallmarks of cynicism is the sense that nothing changes, that we're going to be stuck in the same stupidity of our own making forever. But none of us has a crystal ball. We don't know what the future holds and how humanity will change through the inevitable ups and downs on the horizon. We couldn't have predicted we'd be here now three years ago, and we don't know what things will look like three years from now.

We can choose to envision a dystopian future—there are plenty of books and movies we can use for inspiration if that's what we want to do. Or we can choose to envision something better or greater than what we have now. Neither is guaranteed in any way, so we do have a choice in the matter.

Any psychologist will tell you that visualization can be a powerful and transformative tool. Just as we see what we look for in the present, we are more likely to create what we envision for the future. That's not to say that we can control everything, but we can decide what direction we try to encourage humanity to go with our lives. When we look forward to a future in which humanity and our planetary home thrive and flourish, we're much more likely to seek out ways to move us in that direction.

Hope is a choice we make daily, in our thoughts and in our actions. Cynicism can sing to us all it wants, but we will hold the wheel steady, look for the light on the horizon and steer that direction instead.

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Three women, three MS journeys: How multiple sclerosis looks different for everyone

Gina, Nathalie and Helga share their reactions to being diagnosed with MS and how they stay informed and positive in the face of ever-changing symptoms.

Courtesy of Sanofi

Helga, Nathalie and Gina all have MS, and their experiences show how differently the disease can manifest.

True

It’s been 155 years since neurologist Jean-Martin Charcot gave the first lecture on a mysterious progressive illness he called “multiple sclerosis.” Since then, we’ve learned a lot. We know MS causes the immune system to attack healthy tissue, including damaging the brain and spinal cord. Resulting symptoms can be debilitating and include fatigue, blurred vision, memory problems and weakness. Huge advancements in our understanding of MS and its underlying causes, as well as treatment advances, have been made in the past few decades, but MS remains a complex and unpredictable reality for the 2.8 million+ people diagnosed around the world.

Ironically, the only real constant for people living with MS is change. There’s no set pattern or standard progression of the disease, so each person’s experience is unique. Some people with MS have mild symptoms that worsen slowly but sometimes improve, while others can have severe symptoms that drastically alter their daily lives.

All people with MS share some things in common, however, such as the need to stay informed on the ever-evolving research, find various lines of support and try to remain hopeful as they continue living with the disease.

To better understand what navigating life with MS really looks like, three women shared their MS stories with us. Their journeys demonstrate how MS can look different for different people and interestingly, how the language used to talk about the disease can greatly impact how people understand their realities.

woman with horse, woman riding horseGina loves riding her horse, Benita.Courtesy of Sanofi

Gina—Hamburg, Germany (diagnosed with relapsing multiple sclerosis in 2017)

When her youngest son was 4 months old, Gina started having problems with her eye. She’d soon learn she was experiencing optic neuritis—her first symptom of MS.

“Immediately after the diagnosis, I looked up facts on MS because I didn’t know anything about it,” Gina says. “And as soon as I knew what could really happen with this disease, I actually got scared.”

As her family’s primary income provider, she worried about how MS would impact her ability to work as a writer and editor. Her family was afraid she was going to end up in a wheelchair. However, for now, Gina’s MS is managed well enough that she still works full-time and is able to be active.

“When I tell somebody that I have MS, they often don't believe me the first time because I don't fulfill any stereotypes,” she says.

Overwhelmed by negative perspectives on living with MS, Gina sought support in the online MS community, which she found to be much more positive.

“I think it’s important to use as many positive words as you can when talking about MS.” It’s important to be realistic while also conveying hope, she says. “MS is an insidious disease that can cause many bad symptoms…that can be frightening, and you can't gloss over it, either.”

To give back to the online community that helped her so much, Gina started a blog to share her story and help others trying to learn about their diagnosis.

Though she deals with fatigue and cognitive dysfunction sometimes, Gina stays active swimming, biking, riding horses and playing with her sons, who are now 11 and 6.

Cognitive dysfunction is common in MS, with over half of people affected. It can impact memory, attention, planning, and word-finding. As with many aspects of MS, some people experience mild changes, while others face more challenges.

Gina says that while there’s still a lot of education about MS needed, she feels positive about the future of MS because there’s so much research being done.

woman in wheelchair holding medal, woman rowingNathalie is an award-winning rower with multiple international titles.Courtesy of Sanofi

Nathalie — Pennes Mirabeau, France (diagnosed with relapsing-remitting multiple sclerosis in 2002)

Nathalie was a teenager and a competitive athlete when she noticed her first symptoms of MS, but it would take four years of “limbo” before she was diagnosed.

“Ultimately, the diagnosis was more of a relief, than a shock,” she says. “Because when you have signs and you don’t know why, it’s worse than knowing, in the end, what you have.”

However, learning more about the disease—and the realities of disease progression—scared her.

“That glimpse of the future was direct and traumatic,” she says. Her neurologist explained that the disease evolves differently for everyone, and her situation might end up being serious or very mild. So, she decided to stop comparing herself to others with MS.

She said to herself, “We’ll see what happens, and you’ll manage it bit by bit.”

By 2005, Nathalie’s MS had progressed to the point of needing a wheelchair. However, that has not dampened her competitive spirit.

Nathalie began her international rowing career in 2009 and has won multiple world titles, including two Paralympic medals—silver in London and bronze in Tokyo. Now, at 42, she still trains 11 times a week. Fatigue can be a problem, and sometimes hard workouts leave her with muscle stiffness and shaking, but she credits her ongoing sports career for helping her feel in tune with her body’s signals.

“Over the years, I’ve learned to listen to my body, letting my body guide when I need to stop and take breaks,” she says.

Nathalie explains that she used to only look backwards because of the initial shock of her diagnosis. In time, she stopped thinking about what she couldn’t do anymore and focused on her future. She now lives in the following mindset: “Even when doors close, don’t miss out on those that open.” Instead of focusing on what she can’t do, she focuses on the opportunities she still has. Right now, this includes her training for the 2024 Paralympic Games in Paris, where she will compete for another rowing medal.

“I only go forward,” she says. “Well, I try, anyway…It’s easy to say, it’s not always easy to do. But that’s what I try to do.”

woman exiting water after swimming, woman with great daneHelga's Great Dane has become a helpful and beloved companion.Courtesy of Sanofi

Helga—Johannesburg, South Africa (diagnosed with relapsing multiple sclerosis in 2010)

When Helga first started having balance issues and numbness in her feet, she chalked it up to her training as a runner. But when the numbness moved to her face, she knew something was wrong. She never guessed it was MS.

“When I was diagnosed, I felt completely overwhelmed and clueless,” Helga says. “I felt that I had nowhere near enough information. I did not know anything about the disease…I had no idea that it was going to be a process of continually monitoring and adjusting your lifestyle.”

In the beginning, Helga’s symptoms developed slowly, and she didn’t appear ill to others. She was even able to run for a few years after her diagnosis, but she couldn’t do marathons anymore, and she began to fall frequently due to balance issues and right-foot dragging. Then her cognition issues became more problematic, especially in her job as a trainer in a printing company.

“My executive function, decision-making and short-term memory were affected to the point that I was eventually medically unfit for work,” she says. She stopped working in 2017.

However, she didn’t stop living life. Even though she could no longer run, she continued to swim competitively. She got a Great Dane puppy and trained him as a service dog to help her walk. She also serves as vice chair of the patient support organization Multiple Sclerosis South Africa, and she advises others who have been diagnosed to join a patient advocacy group as soon as possible to get reliable information and meet others with MS.

Helga says she is “hopeful” about the future of MS. “I must say that I am so grateful that we have all the new medications available, because my life would not be the same if it wasn't for that,” she adds.

Part of how she manages her MS is by looking at the positives.

“If I could tell the world one thing about MS, it would be that MS is an incurable disease of the nervous system, but it's also the greatest teacher of valuing your health, family, friends, and managing change in your life,” she says. “My life is diversified in a way that I never, ever thought it would, and MS has been honestly the greatest teacher.”

Each MS journey is unique – with each person impacted experiencing different struggles, successes, and feelings as they manage this unpredictable disease. But the common thread is clear – there is a critical need for information, support, and hope. We are proud to participate in World MS Day and share these incredible stories of living life while living with MS. To learn more about MS, go to https://www.sanofi.com/why-words-really-matter-when-it-comes-to-multiple-sclerosis.

MAT-GLB-2301642-v1.0-05/2023

This article was sponsored by Sanofi. Participants were compensated when applicable.

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